chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55655520956555210CA13GENIChomozygous798474588
55655563956555640GC42GENIChomozygous798474589
55655610056556101TG36GENIChomozygous798474590
55655687156556872AC34GENIChomozygous798474591
55655739456557395TC53GENIChomozygous798474592
55655883856558839AT29GENIChomozygous798474593
55655903656559037AG20GENIChomozygous798474594
55655949856559499AT27GENIChomozygous798474595
55655986656559867TC31GENIChomozygous798474596
55656006956560070GA34GENICheterozygous798474597
55656016356560164CT33GENICheterozygous798474598
55656024056560241AT27GENICheterozygous798474599
55656075656560757CT49GENICheterozygous798474600
55656078356560784AG22GENICpossibly homozygous798474601
55656080256560803CT29GENICheterozygous798474602
55656081356560814AG29GENICheterozygous798474603
55656093156560932CT38GENIChomozygous798474604
55656100456561005AG27GENIChomozygous798474605
55656114056561141GT16GENIChomozygous798474606
55656189356561894AT45GENICheterozygous798474607
55656190156561902AT43GENICheterozygous798474608
55656208056562081CT26GENIChomozygous798474609
55656254656562547TC18GENIChomozygous798474610
55656318756563188TC29GENIChomozygous798474611
55656330756563308TA33GENIChomozygous798474612
55656435356564354CA31GENIChomozygous798474613
55656514356565144TG23GENIChomozygous798474614
55656521156565212AG31GENIChomozygous798474615
55656583756565838CT21GENIChomozygous798474616
55656616956566170TC29GENIChomozygous798474617
55656621356566214GA31GENIChomozygous798474618